Evidence map›Paper›PMID 36010889›Full record

ArticleCancers2022

Pediatric Precursor B-Cell Lymphoblastic Malignancies: From Extramedullary to Medullary Involvement.

Emma Kroeze, Laura Arias Padilla, Max Bakker, Judith M Boer, Melanie M Hagleitner, Birgit Burkhardt, Takeshi Mori, Andishe Attarbaschi, Jaime Verdú-Amorós, Marta Pillon and 11 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.4field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 14 citations in OpenAlex.

  1. An unusual cranial manifestation of B-cell precursor lymphoblastic lymphoma in 10-year-old girl.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors at 13 institutions in 14 countries.

Emma KroezePrincess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.ORCID 0000-0002-4258-1291
Laura Arias PadillaNHL-BFM Study Center and Pediatric Hematology and Oncology, University Hospital Muenster, 48149 Muenster, Germany.
Max BakkerPrincess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.
Judith M BoerPrincess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.ORCID 0000-0003-4848-7789
Melanie M HagleitnerPrincess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.
Birgit BurkhardtNHL-BFM Study Center and Pediatric Hematology and Oncology, University Hospital Muenster, 48149 Muenster, Germany.ORCID 0000-0002-1151-829X
Takeshi MoriDepartment of Hematology and Oncology, Hyogo Prefectural Kobe Children's Hospital, Kobe 650-0047, Japan.ORCID 0000-0003-0029-7265
Andishe AttarbaschiDepartment of Pediatric Hematology and Oncology, St. Anna Children's Hospital, Medical University of Vienna, 1090 Vienna, Austria.ORCID 0000-0002-9285-6898
Jaime Verdú-AmorósPediatric Oncology Department, Hospital Clínico Universitario de Valencia, 46010 Valencia, Spain.
Marta PillonClinic of Pediatric Hemato-Oncology, Department of Women's and Children's Health, University of Padova, 46010 Padova, Italy.ORCID 0000-0002-1190-3198
Liliya AnderzhanovaDmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology, 117198 Moscow, Russia.
Edita KabíčkováDepartment of Pediatric Hematology and Oncology, Charles University, 2nd Medical School and University Hospital Motol, 150 06 Prague, Czech Republic.
Alan K S ChiangDepartment of Pediatrics and Adolescent Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Queen Mary Hospital, Pokfulam, Hong Kong.ORCID 0000-0002-1089-5325
Rejin KebudiDivision of Pediatric Hematology-Oncology, Istanbul University, Oncology Institute, 34452 İstanbul, Turkey.ORCID 0000-0003-4344-8174
Karin MellgrenDepartment of Pediatric Oncology, Sahlgrenska University Hospital, University of Gothenburg, 413 45 Gothenburg, Sweden.
Jelena LazicDepartment for Hematology and Oncology, University Children's Hospital, University of Belgrade, 11000 Belgrade, Serbia.ORCID 0000-0002-7495-2069
Janez JazbecDivision of Pediatrics, Hematology and Oncology, University Medical Center Ljubljana, SI-1000 Ljubljana, Slovenia.ORCID 0000-0002-7426-1591
Jules P P MeijerinkPrincess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.ORCID 0000-0002-6860-798X
Auke BeishuizenPrincess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.
Jan L C LoeffenPrincess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.
European Intergroup for Childhood Non-Hodgkin Lymphoma (EICNHL) and the International Berlin–Frankfurt–Münster (i-BFM) Study
Princess Máxima Center · NLUniversity Hospital Münster · DECharles University · CZDmitry Rogachev National Research Center of Pediatric Hematology, Oncology and Immunology · RUHospital Clínico Universitario de Valencia · ESIstanbul University · TRKobe Children's Hospital · JPLjubljana University Medical Centre · SIQueen Mary Hospital · CNSahlgrenska University Hospital · SESt Anna Children's Hospital · ATUniversity of Belgrade · RSUniversity of Padua · IT

Funding

Foundation KiKa 393
6 · The paper itself

Abstract

B-cell lymphoblastic lymphoma (BCP-LBL) and B-cell acute lymphoblastic leukemia (BCP-ALL) are the malignant counterparts of immature B-cells. BCP-ALL is the most common hematological malignancy in childhood, while BCP-LBL accounts for only 1% of all hematological malignancies in children. Therefore, BCP-ALL has been well studied and treatment protocols have changed over the last decades, whereas treatment for BCP-LBL has stayed roughly the same. Clinical characteristics of 364 pediatric patients with precursor B-cell malignancies were studied, consisting of BCP-LBL (n = 210) and BCP-ALL (n = 154) patients. Our results indicate that based on the clinical presentation of disease, B-cell malignancies probably represent a spectrum ranging from complete isolated medullary disease to apparent complete extramedullary disease. Hepatosplenomegaly and peripheral blood involvement are the most important discriminators, as both seen in 80% and 95% of the BCP-ALL patients and in 2% of the BCP-LBL patients, respectively. In addition, we show that the overall survival rates in this cohort differ significantly between BCP-LBL and BCP-ALL patients aged 1−18 years (p = 0.0080), and that the outcome for infants (0−1 years) with BCP-LBL is significantly decreased compared to BCP-LBL patients of all other pediatric ages (p < 0.0001).

Indexed as

B-cell acute lymphoblastic leukemiaB-cell lymphoblastic lymphomaBCP-ALLBCP-LBLdisease spectrumNHLnon-Hodgkin lymphoma

Identifiers

PMID36010889
PMCPMC9405801
OpenAlexW4291415519

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.